Cape Town - 2026 ISMRM-ISMRT Annual Meeting and Exhibition • 09-14 May 2026

Oral

Next-Generation Neuroimaging for Alzheimer’s Disease: From Molecules to Networks

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Next-Generation Neuroimaging for Alzheimer’s Disease: From Molecules to Networks
Oral
Neuro A
Thursday, 14 May 2026
Ballroom West
16:00 - 17:50
Moderators: Xingfeng Shao & Qiuting Wen
Session Number: 605-03
CME/CE Credit Available
This session highlights cutting‑edge MRI and PET-MRI approaches to Alzheimer’s disease, spanning molecular pathology, cerebral blood flow, metabolism, myelin, iron, and neuroinflammation. Together, these studies advance biomarkers and predictive models that illuminate disease progression, resilience, and clinically actionable imaging across the Alzheimer’s spectrum.
Skill Level: Intermediate

16:00 Figure 605-03-001.  Back to the Future: Predicting Individual Tau Progression in Alzheimer's Disease
Robin Sandell, Kamalini Ranasinghe, Srikantan Nagarajan, Ashish Raj
University of California San Francisco, San Francisco, United States of America
Impact: A novel computational framework enables clinicians to forecast individual tau progression from single MRI/PET visits, facilitating personalized treatment planning and clinical trial stratification. Predicting future pathology patterns from baseline scans could transform precision medicine approaches in neurodegenerative disease management.
16:11 Figure 605-03-002.  Improving Amyloid Detection and Brain PET Image Quality Using MR-Guided Reconstruction on Integrated PET/MR
AMPC Selected
Yu Cai, Chen Lin, Manoj Jain, Robert Pooley, Jun Zhang, Brittany Benson, Matthew Spangler-Bickell, Alex Smith, Vivek Gupta, Catherine Bullock, Erik Middlebrooks, Neetu Soni
Zhongda Hospital, School of Medicine, Southeast University, China
Impact: MR-guided PET reconstruction enhances reader consistency, confidence, and diagnostic performance in amyloid PET/MR. This technique provides a reliable framework for amyloid PET diagnosis, potentially improving early detection and supporting the monitoring of anti-amyloid therapies in Alzheimer’s disease.
16:22 Figure 605-03-003.  Cerebral blood flow decline in neurodegeneration using a healthy reference normative model
Summa Cum Laude
Mathijs Dijsselhof, David Van Nederpelt, Wibeke Nordhøy, Ole Andreassen, Lars Westlye, Luigi Lorenzini, Leo Pieperhoff, Alle Meije Wink, Floor Duits, Alun Hughes, Jonathan Schott, Menno Schoonheim, Eva Strijbis, Joost Kuijer, Bert-Jan Van den Born, Mervin Tee, Saima Hilal, Christopher Chen, Frederik Barkhof, James Cole, Jan Petr, Henk Mutsaerts
Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands
Impact: Charting healthy reference life-course cerebral blood flow (CBF) and its deviations in cerebrovascular and neurodegenerative pathology will aid in developing early (cerebro)vascular-based diagnosis and personalised preventative and treatment strategies, advancing CBF as a non-invasive generalisable physiological cerebrovascular biomarker.
16:33 Figure 605-03-004.  Dynamic Deuterium Metabolic Imaging in Patients with Alzheimer’s Disease at 3T: Initial Feasibility Study
Yang Fan, Jialu Zhang, Jinxia Guo, Chunsheng Wang, Rolf Schulte, Bing Wu, Feng Chen
GE Healthcare, Beijing, China
Impact: Dynamic DMI at 3T enables time‑resolved mapping of cerebral glucose metabolism in Alzheimer’s disease patients. This pilot study establishes feasibility and highlights potential for a radiation‑free biomarker to monitor neurodegeneration and therapeutic response.

16:44 Figure 605-03-005.  Glial metabolic alterations in an Alzheimer’s disease model with selective ApoE4-to-ApoE2 switching in the brain
Magna Cum Laude
Tamara Vasilkovska, Aditya Jhajharia, Xiao Gao, Georgios Batsios, Minjie Zhu, Lesley Golden, Georgia Nolt, Ken Nakamura, Pavithra Viswanath, Lance Johnson, Jeremy Gordon
University Of California, San Francisco (UCSF), United States of America
Impact: This study shows the potential of using hyperpolarized (HP) 13C MRI to investigate in-vivo, in real-time metabolic alterations in Alzheimer’s disease (AD). Importantly, this work shows the application of HP 13C MRI in understanding cell-specific therapeutic strategies in AD.
16:55 Figure 605-03-006.  Limbic Neurometabolic Network Segregation Underlies Cognitive Resilience in Alzheimer’s Disease
Summa Cum Laude AMPC Selected
Wenli Li, Miao Zhang, Yibo Zhao, Yudu Li, Wen Jin, Yaoyu Zhang, Yue Guan, Wenqi Zhang, Zhi-Pei Liang, Yao Li
Shanghai Jiao Tong University, Shanghai, China
Impact: Neurometabolic network segregation within the limbic system underlies cognitive resilience in AD. Preserved neuronal network organization may buffer against glucose hypometabolism, offer potential biomarkers and provide targets for interventions aimed at maintaining cognition despite AD pathology.
17:06 Figure 605-03-007.  Clinically feasible SANDI MRI for early identification of neurodegeneration in Alzheimer’s disease
Summa Cum Laude
Hansol Lee, Jeremy Ford, Kwok-Shing Chan, Hong Hsi Lee, Susie Huang
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, United States of America
Impact: Clinical SANDI enables early, noninvasive detection of AD-related microstructural changes using clinically feasible multi-shell diffusion MRI. Its high sensitivity and clinical applicability highlight its practical utility, with strong translational potential to advance understanding of AD pathophysiology and its clinical implications.
17:17 Figure 605-03-008.  Direct Myelin Imaging as a Novel Biomarker Across the Alzheimer Disease Spectrum
Jinil Park, Sam Sedaghat, Brittany Dugger, Eddie Fu, Kader Oguz, Youngkyoo Jung, Fang Liu, Hyungseok Jang
University of California, Berkeley, United States of America
Impact: This work demonstrates Inversion Recovery Ultrashort Echo Time (IR-UTE) MRI technique to assess myelin integrity in human post-mortem brain tissues. This provides a feasible imaging biomarker to assess demyelination, a critical early event in Alzheimer disease, and track its progression.
17:28 Figure 605-03-009.  Gradient Echo with Improved Microstructure-Informed Myelin, Iron and Water Mapping predicts Cognitive Decline in Aging and AD
Magna Cum Laude
MANXI XU, Mert Sisman, Aocai Yang, Yian Gao, Peiling Ou, Pascal Spincemaille , Guolin Ma, Yi Wang
China-Japan Friendship Hospital, Beijing, China
Impact: This study highlights iMIMM's ability to noninvasively detect white matter changes like myelin loss, iron alterations, and edema in cognitive decline, offering potential biomarkers for early AD detection and personalized interventions, advancing MRI-based neurological assessments.
17:39 Figure 605-03-010.  Quantitative Susceptibility Mapping Detects Neuroinflammation-Driven Changes Across the Alzheimer’s Disease Continuum
Seyyed Ali Hosseini, Nesrine Rahmouni, Stijn Servaes, Arthur C. Macedo, Tevy Chan, Brandon Hall, Hangwei Zhuang, Junghun Cho, Sanjeev Chawla, Yi Wang, Pedro Rosa‐Neto
McGill University, Montreal, Canada
Impact: QSM identifies neuroinflammation-linked magnetic susceptibility alterations independent of amyloid and tau pathology. These findings provide a clinically practical, radiation-free biomarker to evaluate disease-modifying therapies targeting iron dysregulation and microglial activation in Alzheimer’s disease.

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